Entropy
Temperature
Internal energy
Enthalpy
D. Enthalpy
Adiabatic process
Endothermic reaction
Exothermic reaction
Process involving a chemical reaction
2.73
28.3
273
283
SO2
NH3
CCl2F2
C2H4Cl2
Always exists
May exist
Never exists
Is difficult to predict
dE = CpdT
dE = CvdT
dQ = dE + pdV
dW = pdV
μ° + RT ln f
μ°+ R ln f
μ° + T ln f
μ° + R/T ln f
Cp/Cv
Cp/(CP-R)
1 + (R/CV)
All (A), (B) and (C)
Increase
Decrease
Remain same
Increase in summer and will decrease in winter
Fusion
Vaporisation
Transition
None of these
Phase rule variables are intensive properties
Heat and work are both state function
The work done by expansion of a gas in vacuum is zero
CP and CV are state function
(∂P/∂V)T
(∂V/∂T)P
(∂P/∂V)V
All (A), (B) & (C)
12 P1V1
6 P1 V1
3 P1V1
P1 V1
Increases
Decreases
Remains unchanged
May increase or decrease; depends on the substance
Positive
Negative
Zero
May be positive or negative
States that n1dμ1 + n2dμ2 + ....njdμj = 0, for a system of definite composition at constant temperature and pressure
Applies only to binary systems
Finds no application in gas-liquid equilibria involved in distillation
None of these
Pressure
Temperature
Both (A) & (B)
Neither (A) nor (B)
Equal to its density
The reciprocal of its density
Proportional to pressure
None of these
It should be non-explosive
It should have a sub-atmospheric vapor pressure at the temperature in refrigerator coils
Its vapor pressure at the condenser temperature should be very high
None of these
In which there is a temperature drop
Which is exemplified by a non-steady flow expansion
Which can be performed in a pipe with a constriction
In which there is an increase in temperature
Initial concentration of the reactant
Pressure
Temperature
None of these
The surface tension vanishes
Liquid and vapour have the same density
There is no distinction between liquid and vapour phases
All (A), (B) and (C)
1
< 1
> 1
Either (B) or (C), depends on the nature of the gas
System and surroundings pressure be equal
Friction in the system should be absent
System and surroundings temperature be equal
None of these
Number of intermediate chemical reactions involved
Pressure and temperature
State of combination and aggregation in the beginning and at the end of the reaction
None of these
(dF)T, p < 0
(dF)T, p > 0
(dF)T, p = 0
(dA)T, v < 0
ds = 0
ds < 0
ds > 0
ds = Constant
d ln p/dt = Hvap/RT2
d ln p/dt = RT2/Hvap
dp/dt = RT2/Hvap
dp/dt = Hvap/RT2
(∂T/∂V)S, ni = -(∂P/∂S)V, ni
(∂S/∂P)T, ni = (∂V/∂T)P, ni
(∂S/∂V)T, ni = (∂P/∂T)V, ni
(∂T/∂P)S, ni = (∂V/∂S)P, ni
[∂(G/T)/∂T] = - (H/T2)
[∂(A/T)/∂T]V = - E/T2
Both (A) and (B)
Neither (A) nor (B)
The conversion for a gas phase reaction increases with decrease in pressure, if there is an increase in volume accompanying the reaction
With increase in temperature, the equilibrium constant increases for an exothermic reaction
The equilibrium constant of a reaction depends upon temperature only
The conversion for a gas phase reaction increases with increase in pressure, if there is a decrease in volume accompanying the reaction